Canonical Allele Identifier: CA2631005471
Gene: TELO2 HGNC NCBI

Linked Data

gnomAD v4: 16-1510234-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1510234A>G , CM000678.2:g.1510234A>G GRCh38
NC_000016.9:g.1560235A>G , CM000678.1:g.1560235A>G GRCh37
NC_000016.8:g.1500236A>G NCBI36
NG_032783.1:g.106875T>C
NG_050910.1:g.21891A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262319.11:c.*298A>G MANE Select ENSP00000262319.6:n.*298A>G
ENST00000262319.10:c.*298A>G ENSP00000262319.6:n.*298A>G
ENST00000568240.1:n.1104A>G
NM_016111.3:c.*298A>G NP_057195.2:n.*298A>G
XM_011522773.1:c.*298A>G XP_011521075.1:n.*298A>G
XM_011522774.1:c.*298A>G XP_011521076.1:n.*298A>G
XM_011522775.1:c.*298A>G XP_011521077.1:n.*298A>G
XM_011522776.1:c.*298A>G XP_011521078.1:n.*298A>G
XR_932982.1:n.3111A>G
NM_001351846.1:c.*298A>G NP_001338775.1:n.*298A>G
XM_011522773.3:c.*298A>G XP_011521075.1:n.*298A>G
XM_011522774.2:c.*298A>G XP_011521076.1:n.*298A>G
XM_011522775.3:c.*298A>G XP_011521077.1:n.*298A>G
XM_011522776.2:c.*298A>G XP_011521078.1:n.*298A>G
XR_001752042.2:n.3344A>G
XR_001752043.2:n.2859A>G
XR_001752044.2:n.2796A>G
XR_932982.3:n.2889A>G
NM_016111.4:c.*298A>G MANE Select NP_057195.2:n.*298A>G
NM_001351846.2:c.*298A>G NP_001338775.1:n.*298A>G